BEUDAMED
    6 results · 28ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    ACCU-FLO REGULATOR

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    SG-066 OXYGEN ENRICHMENT KIT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ANGIOMED HARZMANN DISCS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2014

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·October 6, 2010

    DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·December 10, 2012